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eConsentCloudbyz

Cloudbyz eConsent is a cloud-based solution that replaces paper-based informed consent with interactive, multimedia-enabled, and template-driven digital consent on mobile devices, enhancing participant comprehension, engagement, and compliance while streamlining workflows for sponsors, CROs, and sites.

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Product details

eConsent

Cloudbyz eConsent is a cloud-based solution built on the Salesforce platform that replaces traditional paper-based informed consent with an interactive, multimedia-enabled, and template-driven digital experience. Designed for sponsors, CROs, and sites, it enhances participant comprehension, engagement, and compliance while streamlining workflows and improving operational efficiency across clinical trials.

Features

  • Interactive Multimedia Presentation: Uses videos, graphics, and dynamic content to explain study procedures and improve understanding.
  • Participant Engagement Tools: Enables participants to ask questions via chat or highlight unclear text, with saved threads for future reference.
  • Compliance Quizzes: Includes quizzes at various stages to assess participant comprehension and track responses.
  • Electronic Signature Workflows: Standardized e-signature processes with audit trails and version control.
  • Template-Based Consent Forms: Create reusable templates and ICF checklists for consistent documentation across studies.
  • Secure Document Upload: Participants can upload identity documents securely with end-to-end encryption.
  • Multi-language & Accessibility Support: Offers language selection and text sizing for global trials and diverse populations.
  • OTP Login & Verification: Supports secure access via One-Time Passcodes for remote and mobile use.

Capabilities

  • Real-Time Collaboration: Enables study teams to monitor consent progress and participant feedback instantly.
  • Audit-Ready Compliance: Built-in support for HIPAA and 21 CFR Part 11 with full traceability.
  • Participant-Centric Design: Reduces drop-out rates by allowing participants to complete consent remotely and at their own pace.
  • Customizable Consent Workflows: Adaptable to different study protocols and regulatory requirements.
  • Analytics & Metrics Tracking: Provides insights into participant comprehension and consent process efficiency.
  • Scalable for Global Trials: Supports multilingual and multi-site deployments with centralized management.

Benefits

  • Improves participant understanding and engagement through interactive content.
  • Reduces administrative burden and site visits with remote consent capabilities.
  • Enhances compliance and data quality with standardized workflows and audit trails.
  • Accelerates study start-up and onboarding with reusable templates and automation.
  • Increases transparency and trust between participants and study teams.
  • Supports global operations with multilingual and mobile-friendly interfaces.
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